000 | 01960nam a22002417a 4500 | ||
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003 | ISI Library, Kolkata | ||
005 | 20240806151230.0 | ||
008 | 240806b |||||||| |||| 00| 0 eng d | ||
020 | _a9241207604 | ||
040 |
_aISI Library _bEnglish |
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082 | 0 | 4 |
_a100 SD;610.621 _bWHO.TR.760 |
110 | 1 | _aWHO Expert Committee on Biological Standardization | |
245 | 1 | 0 |
_aWHO Expert Committee on Biological Standardization : _bthirty-seventh report, meeting held in Geneva from 1 to 8 December 1986 |
260 |
_aGeneva : _bWorld Health Organization, _c1987 |
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300 |
_a203 Pages; _c20 cm. |
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490 | 0 | _aWorld Health Organization technical report series ; no. 760 | |
505 | 0 | _aGeneral -- Substances: Antibiotics -- Antibodies -- Blood products and related substances -- Endocrinological and related substances -- Miscellaneous -- requirements for biological substances -- Annaxes | |
520 | _aAnnounces changes in the status or development of international standards for 35 biologicals, classified as antibiotics, antibodies, antigens, blood products and related substances, endocrinological and related substances, and a miscellaneous group of substances. The report also provides detailed information on requirements for the manufacturing, testing, and quality control of selected vaccines, including hepatitis B vaccines made by recombinant DNA techniques in yeast, live mumps vaccine, and inactivated rabies vaccine produced in continuous cell lines. Of particular practical interest is an extensive report on a WHO meeting concerned with the use of recombinant DNA techniques to produce hepatitis B vaccines. The report also includes amendments to previous requirements for oral poliomyelitis vaccine and for diphtheria toxoid, pertussis vaccine, tetanus toxoid, and combined vaccines. | ||
650 | 4 | _aBiological Products | |
650 | 4 | _aPharmacology, Toxicology and Clinical Technology | |
710 | 1 | _aWorld Health Organization | |
942 |
_2ddc _cRP |
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999 |
_c435595 _d435595 |